Canonical Allele Identifier: CA412548021
Gene: NR0B1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.30326760C>A (hg19) chrX:g.30308643C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.30308643C>A , CM000685.2:g.30308643C>A GRCh38
NC_000023.10:g.30326760C>A , CM000685.1:g.30326760C>A GRCh37
NC_000023.9:g.30236681C>A NCBI36
NG_009814.1:g.5736G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378970.5:c.721G>T MANE Select ENSP00000368253.4:p.Gly241Cys
ENST00000378970.4:c.721G>T ENSP00000368253.4:p.Gly241Cys
NM_000475.4:c.721G>T NP_000466.2:p.Gly241Cys
NM_000475.5:c.721G>T MANE Select NP_000466.2:p.Gly241Cys
Search 100 bp 5'
Search 100 bp 3'